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1 ery rare human genetic disorder, restrictive dermopathy.
2 c27a4 to be a candidate gene for restrictive dermopathy.
3        Thyroid-associated ophthalmopathy and dermopathy are connective tissue manifestations of Grave
4 ear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy.
5 e and those in the pretibial skin, localized dermopathy, has yet to be established.
6                        Nephrogenic fibrosing dermopathy (NFD) is a newly recognized cutaneous fibroti
7                        Nephrogenic fibrosing dermopathy (NFD) is a newly recognized scleroderma-like
8 the severe laminopathy diseases, restrictive dermopathy (RD) and Hutchinson Gilford progeria syndrome
9                                  Restrictive dermopathy (RD) is a lethal human genetic disorder chara
10  more severe progeroid disorder, restrictive dermopathy (RD), is caused by the loss of the prelamin A
11 ord progeria syndrome (HGPS) and restrictive dermopathy (RD), premature aging is linked to accumulati
12 e progeria (atypical 'HGPS') and restrictive dermopathy (RD).
13 sing a severe progeroid disease, restrictive dermopathy (RD).
14 al perinatal progeroid syndrome: restrictive dermopathy (RD).
15 ibrosis, also known as nephrogenic fibrosing dermopathy, was first documented in 1997 as a scleroderm

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